Details
Stereochemistry | RACEMIC |
Molecular Formula | C26H31Cl2N5O3 |
Molecular Weight | 532.462 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)N1CCN(CC1)C2=CC=C(OC[C@@H]3CO[C@](CN4C=NC=N4)(O3)C5=C(Cl)C=C(Cl)C=C5)C=C2
InChI
InChIKey=BLSQLHNBWJLIBQ-ZEQKJWHPSA-N
InChI=1S/C26H31Cl2N5O3/c1-19(2)31-9-11-32(12-10-31)21-4-6-22(7-5-21)34-14-23-15-35-26(36-23,16-33-18-29-17-30-33)24-8-3-20(27)13-25(24)28/h3-8,13,17-19,23H,9-12,14-16H2,1-2H3/t23-,26-/m1/s1
Molecular Formula | C26H31Cl2N5O3 |
Molecular Weight | 532.462 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/019579s037,019641s030,019964s032lbl.pdfCurator's Comment: description was created based on several sources, including
http://reference.medscape.com/drug/terazol-3-terconazole-vaginal-342596 | https://www.drugs.com/cdi/terconazole-cream.html | https://www.drugbank.ca/drugs/DB00251 | https://www.ncbi.nlm.nih.gov/pubmed/3891537
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/019579s037,019641s030,019964s032lbl.pdf
Curator's Comment: description was created based on several sources, including
http://reference.medscape.com/drug/terazol-3-terconazole-vaginal-342596 | https://www.drugs.com/cdi/terconazole-cream.html | https://www.drugbank.ca/drugs/DB00251 | https://www.ncbi.nlm.nih.gov/pubmed/3891537
Terconazole is an antifungal drug used to treat vaginal yeast infection. Terconazole may exert its antifungal activity by disrupting normal fungal cell membrane permeability. Terconazole and other triazole antifungal agents inhibit cytochrome P450 "14-alpha-demethylase" in susceptible fungi, which leads to the accumulation of lanosterol and other methylated sterols and a decrease in ergosterol concentration. Depletion of ergosterol in the membrane disrupts the structure and function of the fungal cell leading to a decrease or inhibition of fungal growth. During controlled clinical studies conducted in the United States, 521 patients with vulvovaginal candidiasis were treated with terconazole 0.4% vaginal cream. Based on comparative analyses with placebo, the adverse experiences considered most likely related to terconazole 0.4% vaginal cream were a headache and body pain. Fever and chills, vulvovaginal burning, itching, and irritation have also been reported. The adverse drug experience on terconazole most frequently causing discontinuation was vulvovaginal itching.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL3401 Sources: https://www.ncbi.nlm.nih.gov/pubmed/20966043 |
8.9 µM [EC50] | ||
Target ID: CHEMBL1780 Sources: https://www.ncbi.nlm.nih.gov/pubmed/17194716 |
3.0 µM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Curative | TERAZOL 7 Approved UseTerconazole vaginal cream 0.4% is indicated for the local treatment of vulvovaginal candidiasis (moniliasis). As terconazole vaginal cream 0.4% is effective only for vulvovaginitis caused by the genus Candida, the diagnosis should be confirmed by KOH smears and/or cultures. Launch Date1987 |
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Preventing | TERAZOL 7 Approved UseTerconazole vaginal cream 0.4% is indicated for the local treatment of vulvovaginal candidiasis (moniliasis). As terconazole vaginal cream 0.4% is effective only for vulvovaginitis caused by the genus Candida, the diagnosis should be confirmed by KOH smears and/or cultures. Launch Date1987 |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
5.9 ng/mL |
40 mg 1 times / day multiple, vaginal dose: 40 mg route of administration: Vaginal experiment type: MULTIPLE co-administered: |
TERCONAZOLE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
6.9 h |
30 mg single, oral dose: 30 mg route of administration: Oral experiment type: SINGLE co-administered: |
TERCONAZOLE plasma | Homo sapiens population: UNKNOWN age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
Funbound
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
5.1% |
TERCONAZOLE plasma | Homo sapiens population: UNKNOWN age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
Doses
Dose | Population | Adverse events |
---|---|---|
0.8 % 1 times / day multiple, vaginal Recommended Dose: 0.8 %, 1 times / day Route: vaginal Route: multiple Dose: 0.8 %, 1 times / day Sources: |
unhealthy, adult n = 243 Health Status: unhealthy Condition: vulvovaginal candidiasis Age Group: adult Sex: F Population Size: 243 Sources: |
Disc. AE: Allergic reaction, Vaginitis... AEs leading to discontinuation/dose reduction: Allergic reaction Sources: Vaginitis |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Allergic reaction | Disc. AE | 0.8 % 1 times / day multiple, vaginal Recommended Dose: 0.8 %, 1 times / day Route: vaginal Route: multiple Dose: 0.8 %, 1 times / day Sources: |
unhealthy, adult n = 243 Health Status: unhealthy Condition: vulvovaginal candidiasis Age Group: adult Sex: F Population Size: 243 Sources: |
Vaginitis | Disc. AE | 0.8 % 1 times / day multiple, vaginal Recommended Dose: 0.8 %, 1 times / day Route: vaginal Route: multiple Dose: 0.8 %, 1 times / day Sources: |
unhealthy, adult n = 243 Health Status: unhealthy Condition: vulvovaginal candidiasis Age Group: adult Sex: F Population Size: 243 Sources: |
PubMed
Title | Date | PubMed |
---|---|---|
Prediction of genotoxicity of chemical compounds by statistical learning methods. | 2005 Jun |
|
Enantioselective separation of azole compounds by EKC. Reversal of migration order of enantiomers with CD concentration. | 2007 Aug |
|
5-(4-Chloro-phen-yl)-3-(2,4-dimethyl-thiazol-5-yl)-1,2,4-triazolo[3,4-a]isoquinoline. | 2010 Apr 10 |
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Chromatographic and electrophoretic techniques used in the analysis of triazole antifungal agents-a review. | 2010 Sep 15 |
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Profiling of a prescription drug library for potential renal drug-drug interactions mediated by the organic cation transporter 2. | 2011 Jul 14 |
|
Elucidating mechanisms of toxicity using phenotypic data from primary human cell systems--a chemical biology approach for thrombosis-related side effects. | 2015 Jan 5 |
Sample Use Guides
One full applicator (5 g) of TERAZOL® 7 Vaginal Cream (20 mg terconazole) should be administered intravaginally once daily at bedtime for seven consecutive days.
One full applicator (5 g) of TERAZOL® 3 Vaginal Cream (40 mg terconazole) should be administered intravaginally once daily at bedtime for three consecutive days.
One TERAZOL® 3 Vaginal Suppository (80 mg terconazole) should be administered intravaginally once daily at bedtime for three consecutive days.
Route of Administration:
Vaginal
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3891537
Terconazole was dissolved in methyl alcohol to a final concentration of 250 mkg/ml. 20 mkl of these solutions were added to 6 mm blank antibiotic discs (BBL) and dried at room temperature to yield 5 mkg/disk. The disks were applied to the inoculated surface of a two-layer agar assay plate (150 mm dia.). The base uninoculated layer contained 42 ml of the supplemented agar selected for the study. The agar selected was TSA containing 16 mkg/ml biotin, sodium chloride. 1.5% (w/v), pH 7.4. The inoculated top layer consisted of 8 ml of the same agar. The final cell count was 6.4 X 10^4 colony-forming units (CFU)/ml of agar. Within 30 min of preparation of the agar plate, disks of each of the test compounds were placed on the agar surface and the plates incubated 48 h at 37.5 °C. The zones of inhibition were measured to the nearest 0.5 mm
Substance Class |
Chemical
Created
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admin
on
Edited
Fri Dec 15 18:05:23 GMT 2023
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Record UNII |
0KJ2VE664U
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Record Status |
Validated (UNII)
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WHO-VATC |
QG01AG02
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WHO-ATC |
G01AG02
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NCI_THESAURUS |
C514
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NDF-RT |
N0000008217
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NDF-RT |
N0000175487
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267-751-6
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9451
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100000082687
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DB00251
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Terconazole
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1643703
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67915-31-5
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m10573
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TERCONAZOLE
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CHEMBL1306
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SUB10917MIG
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C037815
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480953
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DTXSID2045498
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4815
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331942
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0KJ2VE664U
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0KJ2VE664U
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2599
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37806
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C29493
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IMPURITY -> PARENT |
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USP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
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ACTIVE MOIETY |